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Details Top

Internal ID UUID64405251d60b2039399051
Scientific name Plicanthus hirtellus
Authority (F.Weber) R.M.Schust.
First published in Nova Hedwigia 74: 492 2002

Description Top

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Synonyms Top

Scientific name Authority First published in
Jungermannia hirtella F.Weber Hist. Musc. Hepat. Prodr. 50 1815
Temnoma hirtellum (F.Weber) S.Hatt. J. Hattori Bot. Lab. 7: 47 1952
Anthelia hirtella (F.Weber) Stephani Rev. Bryol. 18: 56

Common names Top

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Language Common/alternative name
Chinese 齿边褶萼苔
Chinese 齒邊褶萼苔

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001209199
Tropicos 35210526
INPN 657392
The Plant List tro-35210526
Open Tree Of Life 428570
NCBI Taxonomy 264783
Nature Serve 2.127828
iNaturalist 567002
GBIF 2689411

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Plant virus movement proteins originated from jelly-roll capsid proteins Butkovic A, Dolja VV, Koonin EV, Krupovic M PLoS Biol 15-Jun-2023
PMCID:PMC10306228
doi:10.1371/journal.pbio.3002157
PMID:37319262
Liverwort and Hornwort Flora of Hoàng Liên National Park and the Adjacent Areas (North Vietnam, Indochina) Bakalin VA, Klimova KG, Nguyen VS, Nguyen HM, Bakalin DA, Choi SS Plants (Basel) 29-Apr-2023
PMCID:PMC10181137
doi:10.3390/plants12091841
PMID:37176900
Expanding the Repertoire of the Plant-Infecting Ophioviruses through Metatranscriptomics Data Debat H, Garcia ML, Bejerman N Viruses 25-Mar-2023
PMCID:PMC10144540
doi:10.3390/v15040840
PMID:37112821
Volatile Organic Compounds of Bryophytes from Peninsular Malaysia and Their Roles in Bryophytes Koid CW, Shaipulah NF, Lee GE, Gradstein SR, Asakawa Y, Andriani Y, Mohammed A, Norhazrina N, Chia PW, Ramlee MZ Plants (Basel) 29-Sep-2022
PMCID:PMC9573159
doi:10.3390/plants11192575
PMID:36235441
Different Predictors Shape the Diversity Patterns of Epiphytic and Non-epiphytic Liverworts in Montane Forests of Uganda Maul K, Wei YM, Nebel M, Luebert F, Ho BC, Quandt D, Kessler M Front Plant Sci 24-Jun-2020
PMCID:PMC7327462
doi:10.3389/fpls.2020.00765
PMID:32670313
Mitochondrial genomes of the early land plant lineage liverworts (Marchantiophyta): conserved genome structure, and ongoing low frequency recombination Dong S, Zhao C, Zhang S, Zhang L, Wu H, Liu H, Zhu R, Jia Y, Goffinet B, Liu Y BMC Genomics 09-Dec-2019
PMCID:PMC6902596
doi:10.1186/s12864-019-6365-y
PMID:31818248
The First Biflavone Found in Liverworts and Other Phenolics and Terpenoids from Chandonanthus hirtellus ssp. giganteus and Plagiochila asplenioides Ludwig Kraut, Rüdiger Mues Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1999-1-203
Chemotypes and Biomarkers of Seven Species of New Caledonian Liverworts from the Bazzanioideae Subfamily Métoyer B, Lebouvier N, Hnawia E, Herbette G, Thouvenot L, Asakawa Y, Nour M, Raharivelomanana P Molecules 05-Jun-2018
PMCID:PMC6100190
doi:10.3390/molecules23061353
PMID:29874780
Chemical Constituents of Two Liverworts <i>Metacalypogeia Alternifolia</i> and <i>Chandonanthus Hirtellus</i> Horng‐Shing Shy, Chia‐Li Wu, Claudia Paul, Wilfried A. König, Uni‐Juni Ean Wiley 01-May-2015
doi:10.1002/JCCS.200200091
Cembrane-type diterpenoids from the Chinese liverworts Chandonanthus hirtellus and C. birmensis. Li RJ, Lin ZM, Kang YQ, Guo YX, Lv X, Zhou JC, Wang S, Lou HX J Nat Prod 28-Feb-2014
doi:10.1021/NP400936T
PMID:24491225
Zierane sesquiterpene lactone, cembrane and fusicoccane diterpenoids, from the Tahitian liverwort Chandonanthus hirtellus. Komala I, Ito T, Nagashima F, Yagi Y, Kawahata M, Yamaguchi K, Asakawa Y Phytochemistry 01-Aug-2010
doi:10.1016/J.PHYTOCHEM.2010.04.023
PMID:20546815
Terpenoids from the liverwort Chandonanthus hirtellus Yanmei Wang, Leslie J. Harrison, Benito C. Tan Elsevier BV 20-Mar-2009
doi:10.1016/J.TET.2009.03.026
Terpenoids and aromatic compounds from selected East Malaysian liverworts Yoshinori Asakawa, Xuehui Lin, Keiko Kondo, Yoshiyasu Fukuyama Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83456-U

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
4,8,12,15,15-Pentamethylbicyclo[9.3.1]pentadeca-3,7-dien-12-ol 620816 Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)C 290.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(11-Acetyloxy-4,9,12-trimethyl-15-prop-1-en-2-yl-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-2-yl) acetate 163023164 Click to see CC1=CC(C2(CCC(C2C(CC3(C(O3)CC1)C)OC(=O)C)C(=C)C)C)OC(=O)C 404.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
(1R,3aS,4R,5E,9E,12aS)-3a,6,10-trimethyl-1-prop-1-en-2-yl-2,3,4,7,8,11,12,12a-octahydro-1H-cyclopenta[11]annulen-4-ol 162924475 Click to see CC1=CCCC(=CC(C2(CCC(C2CC1)C(=C)C)C)O)C 288.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
(2-Acetyloxy-11-hydroxy-4,9,12-trimethyl-15-prop-1-en-2-yl-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-13-yl) acetate 163045432 Click to see CC1=CC(C2(C(CC(C2C(CC3(C(O3)CC1)C)OC(=O)C)C(=C)C)OC(=O)C)C)O 420.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
[(1S,2S,4S,6S,9E,11R,12R,13S,15R)-2,11-diacetyloxy-4,9,12-trimethyl-15-[(2R)-2-methyloxiran-2-yl]-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-13-yl] acetate 76324846 Click to see CC1=CC(C2(C(CC(C2C(CC3(C(O3)CC1)C)OC(=O)C)C4(CO4)C)OC(=O)C)C)OC(=O)C 478.60 unknown https://doi.org/10.1016/J.TET.2009.03.026
[(1S,2S,4S,6S,9E,11R,12S,13S,15R)-2-acetyloxy-11-hydroxy-4,9,12-trimethyl-15-prop-1-en-2-yl-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-13-yl] acetate 163045433 Click to see CC1=CC(C2(C(CC(C2C(CC3(C(O3)CC1)C)OC(=O)C)C(=C)C)OC(=O)C)C)O 420.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
[(1S,2S,4S,6S,9E,11R,12S,15R)-11-acetyloxy-4,9,12-trimethyl-15-[(2R)-2-methyloxiran-2-yl]-13-oxo-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-2-yl] acetate 162849170 Click to see CC1=CC(C2(C(C(CC2=O)C3(CO3)C)C(CC4(C(O4)CC1)C)OC(=O)C)C)OC(=O)C 434.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
[(1S,2S,4S,6S,9E,11R,12S,15R)-11-acetyloxy-4,9,12-trimethyl-15-prop-1-en-2-yl-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-2-yl] acetate 163023165 Click to see CC1=CC(C2(CCC(C2C(CC3(C(O3)CC1)C)OC(=O)C)C(=C)C)C)OC(=O)C 404.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
[11-Acetyloxy-4,9,12-trimethyl-15-(2-methyloxiran-2-yl)-13-oxo-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-2-yl] acetate 162849169 Click to see CC1=CC(C2(C(C(CC2=O)C3(CO3)C)C(CC4(C(O4)CC1)C)OC(=O)C)C)OC(=O)C 434.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
[2,11-Diacetyloxy-4,9,12-trimethyl-15-(2-methyloxiran-2-yl)-5-oxatricyclo[10.3.0.04,6]pentadec-9-en-13-yl] acetate 162891026 Click to see CC1=CC(C2(C(CC(C2C(CC3(C(O3)CC1)C)OC(=O)C)C4(CO4)C)OC(=O)C)C)OC(=O)C 478.60 unknown https://doi.org/10.1016/J.TET.2009.03.026
3a,6,10-trimethyl-1-prop-1-en-2-yl-2,3,4,7,8,11,12,12a-octahydro-1H-cyclopenta[11]annulen-4-ol 162924474 Click to see CC1=CCCC(=CC(C2(CCC(C2CC1)C(=C)C)C)O)C 288.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Fusicoccane diterpenoids
3-Hydroxy-1,4,8-trimethyl-12-propan-2-yltricyclo[9.3.0.03,7]tetradec-6-en-5-one 14707349 Click to see CC1CCC2C(CCC2(CC3(C1=CC(=O)C3C)O)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
Anadensin 14707350 Click to see CC1CCC2C(CCC2(CC3(C1=CC(=O)C3C)O)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Diploptene 92155 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1002/JCCS.200200091
Hopene b 605866 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1002/JCCS.200200091
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(91)83456-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,4S,6S,8R,13S)-2,6,13-trimethyl-10-propan-2-ylidene-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 163028096 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC4(CCC1(O2)O4)C)C 334.40 unknown https://doi.org/10.1002/JCCS.200200091
(1R,2S,4S,6S,8R,13S)-2,6,13-trimethyl-10-propan-2-ylidene-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 163028095 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC4(CCC1(O2)O4)C)C 334.40 unknown https://doi.org/10.1002/JCCS.200200091
(1S,2R,4R,6S,8R,13R)-2,6,13-trimethyl-10-propan-2-ylidene-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 76313955 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC4(CCC1(O2)O4)C)C 334.40 unknown https://doi.org/10.1021/NP400936T
(1S,2R,4S,6S,8S,13R)-2,6,13-trimethyl-10-propan-2-ylidene-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 163028097 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC4(CCC1(O2)O4)C)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
(1S,2R,7R,10R,11S,13R)-4,7,13-trimethyl-10-propan-2-yl-14-oxatetracyclo[9.2.1.01,5.07,11]tetradec-4-en-2-ol 163084283 Click to see CC1CC23C(CCC2(CC4=C(CC(C14O3)O)C)C)C(C)C 290.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
(1S,2S,4R,6S,8R,13R)-2,6,13-trimethyl-10-propan-2-ylidene-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 76335690 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC4(CCC1(O2)O4)C)C 334.40 unknown https://doi.org/10.1021/NP400936T
(1S,2S,4S,6R,8S,10S,13R)-2,6,13-trimethyl-10-propan-2-yl-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 162993094 Click to see CC1CC2CC3(C(O3)C(=O)C(CCC4(CCC1(O2)O4)C)C(C)C)C 336.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
(1S,2S,4S,6R,8S,13R)-2,6,13-trimethyl-10-propan-2-ylidene-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 163187558 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC4(CCC1(O2)O4)C)C 334.40 unknown https://doi.org/10.1016/J.TET.2009.03.026
(6,10,14-Trimethyl-2-oxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadec-10-en-6-yl) acetate 162945418 Click to see CC1=CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1)(C)OC(=O)C)C 362.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
(E)-alpha-bisabolene 5315468 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83456-U
(Z)-alpha-Bisabolene 5352653 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83456-U
[(1R,3S,5R,10R,12Z,14S)-3,10,14-trimethyl-6-oxo-7-propan-2-ylidene-4,16-dioxatricyclo[11.2.1.03,5]hexadec-12-en-10-yl] acetate 76328403 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC(CC=C1O2)(C)OC(=O)C)C 376.50 unknown https://doi.org/10.1021/NP400936T
[(1R,3S,5R,10R,13R,14S)-13-hydroxy-3,10,14-trimethyl-6-oxo-7-propan-2-ylidene-4,16-dioxatricyclo[11.2.1.03,5]hexadecan-10-yl] acetate 76317495 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC(CCC1(O2)O)(C)OC(=O)C)C 394.50 unknown https://doi.org/10.1021/NP400936T
[(1R,6R,10E,14S)-6,10,14-trimethyl-2-oxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadec-10-en-6-yl] acetate 162945421 Click to see CC1=CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1)(C)OC(=O)C)C 362.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
[(1R,6R,10E,14S)-6,10,14-trimethyl-2,9-dioxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadec-10-en-6-yl] acetate 76310268 Click to see CC1=CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1=O)(C)OC(=O)C)C 376.50 unknown https://doi.org/10.1021/NP400936T
[(1R,6R,10R,14S)-6,10,14-trimethyl-2,9-dioxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadecan-6-yl] acetate 76335688 Click to see CC1CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1=O)(C)OC(=O)C)C 378.50 unknown https://doi.org/10.1021/NP400936T
[(1R,6R,10S,14S)-6,10,14-trimethyl-2,9-dioxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadecan-6-yl] acetate 76313954 Click to see CC1CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1=O)(C)OC(=O)C)C 378.50 unknown https://doi.org/10.1021/NP400936T
[(1R,6R,9R,10E,14S)-9-hydroxy-6,10,14-trimethyl-2-oxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadec-10-en-6-yl] acetate 76332079 Click to see CC1=CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1O)(C)OC(=O)C)C 378.50 unknown https://doi.org/10.1021/NP400936T
[(1S,6S,10E,14R)-6,10,14-trimethyl-2-oxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadec-10-en-6-yl] acetate 76335689 Click to see CC1=CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1)(C)OC(=O)C)C 362.50 unknown https://doi.org/10.1021/NP400936T
[(1S,6S,14R)-6,10,14-trimethyl-2-oxo-3-propan-2-ylidene-15-oxabicyclo[12.1.0]pentadec-10-en-6-yl] acetate 162945419 Click to see CC1=CCCC2(C(O2)C(=O)C(=C(C)C)CCC(CCC1)(C)OC(=O)C)C 362.50 unknown https://doi.org/10.1021/NP400936T
2,6,13-Trimethyl-10-propan-2-yl-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 162993093 Click to see CC1CC2CC3(C(O3)C(=O)C(CCC4(CCC1(O2)O4)C)C(C)C)C 336.50 unknown https://doi.org/10.1016/J.TET.2009.03.026
2,6,13-Trimethyl-10-propan-2-ylidene-7,16,17-trioxatetracyclo[11.2.1.11,4.06,8]heptadecan-9-one 75239045 Click to see CC1CC2CC3(C(O3)C(=O)C(=C(C)C)CCC4(CCC1(O2)O4)C)C 334.40 unknown https://doi.org/10.1002/JCCS.200200091
https://doi.org/10.1016/J.TET.2009.03.026
https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
3-(1,5-Dimethyl-4-hexenyl)-6-methylene-1-cyclohexene 519764 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 204.35 unknown https://doi.org/10.1016/J.TET.2009.03.026
4,7,13-Trimethyl-10-propan-2-yl-14-oxatetracyclo[9.2.1.01,5.07,11]tetradec-4-en-2-ol 163084282 Click to see CC1CC23C(CCC2(CC4=C(CC(C14O3)O)C)C)C(C)C 290.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Anastreptene 91746864 Click to see CC1=CCC2C13C2(CCC4C3C4(C)C)C 202.33 unknown https://doi.org/10.1016/0031-9422(91)83456-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
[(1S,2E,4R,6E,10R)-3,7,11,11-tetramethyl-4-bicyclo[8.1.0]undeca-2,6-dienyl] acetate 162876691 Click to see CC1=CCC(C(=CC2C(C2(C)C)CC1)C)OC(=O)C 262.40 unknown https://doi.org/10.1016/J.TET.2009.03.026
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(3aR,4S,5aS,6R,8aR)-3a-methoxy-1,4,8a-trimethyl-6-propan-2-yl-3,4,5,5a,6,7,8,9-octahydrocyclopenta[f]azulen-2-one 162882449 Click to see CC1CC2C(CCC2(CC3=C(C(=O)CC13OC)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
(3aS,4S,5aS,6R,8aR)-3a-hydroxy-1,4,8a-trimethyl-6-propan-2-yl-3,4,5,5a,6,7,8,9-octahydrocyclopenta[f]azulen-2-one 162977969 Click to see CC1CC2C(CCC2(CC3=C(C(=O)CC13O)C)C)C(C)C 290.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
3a-Hydroxy-1,4,8a-trimethyl-6-propan-2-yl-3,4,5,5a,6,7,8,9-octahydrocyclopenta[f]azulen-2-one 162977968 Click to see CC1CC2C(CCC2(CC3=C(C(=O)CC13O)C)C)C(C)C 290.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
3a-Methoxy-1,4,8a-trimethyl-6-propan-2-yl-3,4,5,5a,6,7,8,9-octahydrocyclopenta[f]azulen-2-one 162882448 Click to see CC1CC2C(CCC2(CC3=C(C(=O)CC13OC)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,5S,10R,13R)-13-methyl-4,9-dimethylidene-2-oxatricyclo[8.3.0.01,5]tridecan-3-one 162892517 Click to see CC1CCC2C13C(CCCC2=C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
13-Methyl-4,9-dimethylidene-2-oxatricyclo[8.3.0.01,5]tridecan-3-one 75239046 Click to see CC1CCC2C13C(CCCC2=C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.TET.2009.03.026
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.TET.2009.03.026
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(1S,2S,4S,6R,8R,9R,13Z,16S)-2,6,9,12,12,16-hexamethyl-7,10,11,19,20-pentaoxapentacyclo[14.2.1.11,4.06,8.09,13]icos-13-ene 163185647 Click to see CC1CC2CC3(C(O3)C4(C(=CCC5(CCC1(O2)O5)C)C(OO4)(C)C)C)C 364.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
(1R,6aalpha)-1,4beta,9abeta-Trimethyl-7beta-isopropyl-1alpha,2alpha:3aalpha,10aalpha-diepoxytetradecahydrodicyclopenta[a,d]cyclooctene 11822871 Click to see CC1CCC2C(CCC2(CC34C1(O3)CC5C4(O5)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
3,10,15-Trimethyl-6-propan-2-yl-14,16-dioxapentacyclo[9.4.1.01,11.03,7.013,15]hexadecane 14707343 Click to see CC1CCC2C(CCC2(CC34C1(O3)CC5C4(O5)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Organoheterocyclic compounds / Oxanes
(1R,3R,6R,7S,10S,11R,14S)-3,10,14-trimethyl-6-propan-2-yl-15-oxatetracyclo[9.4.0.01,14.03,7]pentadecan-12-one 14707342 Click to see CC1CCC2C(CCC2(CC34C1C(=O)CC3(O4)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
(2aR,3S,5aS,6R,8aR,9aR,10aS)-Dodecahydro-3,8a,10a-trimethyl-6-(1-methylethyl)-2H-cyclopenta[6 inverted exclamation marka,7 inverted exclamation marka]cycloocta[1 inverted exclamation marka,2 inverted exclamation marka:1,5]cyclopent[1,2-b]oxiren-2-one 14707341 Click to see CC1CCC2C(CCC2(CC34C1C(=O)CC3(O4)C)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
3,10,14-Trimethyl-6-propan-2-yl-15-oxatetracyclo[9.3.1.01,11.03,7]pentadecan-13-one 14707340 Click to see CC1CCC2C(CCC2(CC34C1(O3)CC(=O)C4C)C)C(C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.023
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Dicranolomin 5469097 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4=C(C=CC(=C4O)O)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O)O 570.50 unknown https://doi.org/10.1515/ZNC-1999-1-203
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1515/ZNC-1999-1-203

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